Literature DB >> 16298269

Treatment of hypertension in chronic kidney disease.

Robert D Toto1.   

Abstract

Chronic kidney disease (CKD) is a major public health problem in the United States. It is estimated that nearly 20 million Americans have some degree of chronic kidney disease defined as an estimated glomerular filtration rate of less than sixty milliliters per minute or evidence of kidney damage by imaging study, biopsy, biochemical testing or urine tests with an estimated glomerular filtration rate more than sixty milliliters per minute. Hypertension is present in more than 80% of patients with CKD and contributes to progression of kidney disease toward end stage (ESRD) as well as to cardiovascular events such as heart attack and stroke. In fact the risk for cardiovascular death in this patient population is greater than the risk for progression to ESRD. Proteinuria is an important co-morbidity in hypertensives with CKD and increase risk of disease progression and cardiovascular events. Treatment of hypertension is therefore imperative. The National Kidney Foundation clinical practice guidelines recommend a blood pressure goal of <130 mmHg systolic and <80 mmHg diastolic for all CKD patients. Recent post-hoc analyses of the Modification of Diet in Renal Disease study indicate that lower blood pressure may provide long-term kidney protection in patients with nondiabetic kidney disease. Specifically a mean arterial pressure <92 mmHg (e.g. 120/80 mmHg) as compared to 102-107 mmHg (e.g. 140/90 mmHg) is associated with reduced risk for ESRD. In most cases achieving this goal requires both non-pharmacologic and pharmacologic intervention. Dietary sodium restriction to no more than 2 grams daily is important. In addition, moderate alcohol intake, regular exercise, weight loss in those with a body mass index greater than 25 kg/M(2) and reduced amount of saturated fat help to reduce blood pressure. The first line pharmacologic intervention should be an angiotensin converting enzyme inhibitor or angiotensin II type 1 receptor blocker in those with diabetes or non-diabetics with more than 200 mg protein/gram creatinine on a random urine sample. For non-diabetics with less than 200 mg protein/gram creatinine on a random urine sample, no specific first-line drug class is recommended. After initial dosing with an ACEi, ARB or other drug, a diuretic should be added to the regimen. Thereafter, beta-blockers, calcium channel blockers, apha blockers and alpha 2 agonists (e.g. clonidine) and finally vasodilators (e.g. minoxidil) should be added to achieve blood pressure goal. Combinations of ACEi and ARB are helpful in reducing proteinuria and may also lower blood pressure further in some some cases. Blood pressure should be monitored closely in hypertensive patients with CKD and both clinic and home blood pressure measurements may help the clinician adjust treatment.

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Year:  2005        PMID: 16298269     DOI: 10.1016/j.semnephrol.2005.05.016

Source DB:  PubMed          Journal:  Semin Nephrol        ISSN: 0270-9295            Impact factor:   5.299


  22 in total

1.  Effective antihypertensive strategies for high-risk patients with diabetic nephropathy.

Authors:  Peter Noel Van Buren; Beverley Adams-Huet; Robert Daniel Toto
Journal:  J Investig Med       Date:  2010-12       Impact factor: 2.895

2.  Management of intradialytic hypertension: old problem, old drug?

Authors:  Emanuela Rizzioli; Elena Incasa; Susanna Gamberini; Roberto Manfredini
Journal:  Intern Emerg Med       Date:  2009-04-15       Impact factor: 3.397

3.  Beneficial effect of aliskiren combined with olmesartan in reducing urinary protein excretion in patients with chronic kidney disease.

Authors:  Takahito Moriyama; Yuki Tsuruta; Chiari Kojima; Mitsuyo Itabashi; Hidekazu Sugiura; Takashi Takei; Tetsuya Ogawa; Keiko Uchida; Ken Tsuchiya; Kosaku Nitta
Journal:  Int Urol Nephrol       Date:  2011-05-28       Impact factor: 2.370

4.  Screening and Recognition of Chronic Kidney Disease in VA Health Care System Primary Care Clinics.

Authors:  Shweta Bansal; Michael Mader; Jacqueline A Pugh
Journal:  Kidney360       Date:  2020-07-09

5.  Ca(2+)-Mg (2+)-dependent ATP-ase activity in hemodialyzed children. Effect of a hemodialysis session.

Authors:  Dorota Polak-Jonkisz; Leszek Purzyc; Danuta Zwolińska
Journal:  Pediatr Nephrol       Date:  2010-09-30       Impact factor: 3.714

Review 6.  Ambulatory blood pressure and cardiovascular risk in chronic kidney disease.

Authors:  Paolo Palatini
Journal:  Curr Hypertens Rep       Date:  2008-04       Impact factor: 5.369

Review 7.  Recent advances in the management of secondary hypertension: chronic kidney disease.

Authors:  Takahiro Masuda; Daisuke Nagata
Journal:  Hypertens Res       Date:  2020-06-17       Impact factor: 3.872

8.  Effects of kimchi supplementation on blood pressure and cardiac hypertrophy with varying sodium content in spontaneously hypertensive rats.

Authors:  Seung-Min Lee; Yoonsu Cho; Hye-Kyung Chung; Dong-Hyuk Shin; Woel-Kyu Ha; Sang-Chul Lee; Min-Jeong Shin
Journal:  Nutr Res Pract       Date:  2012-08-31       Impact factor: 1.926

9.  Computer-assisted imaging algorithms facilitate histomorphometric quantification of kidney damage in rodent renal failure models.

Authors:  Marcin Klapczynski; Gerard D Gagne; Sherry J Morgan; Kelly J Larson; Bruce E Leroy; Eric A Blomme; Bryan F Cox; Eugene W Shek
Journal:  J Pathol Inform       Date:  2012-04-28

10.  Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments.

Authors:  Xin Sheng; Yuting Guan; Ziyuan Ma; Junnan Wu; Hongbo Liu; Chengxiang Qiu; Steven Vitale; Zhen Miao; Matthew J Seasock; Matthew Palmer; Myung K Shin; Kevin L Duffin; Steven S Pullen; Todd L Edwards; Jacklyn N Hellwege; Adriana M Hung; Mingyao Li; Benjamin F Voight; Thomas M Coffman; Christopher D Brown; Katalin Susztak
Journal:  Nat Genet       Date:  2021-08-12       Impact factor: 41.307

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